Canonical Allele Identifier: CA571717722

Gene: PRKN

Linked Data

• dbSNP Id: rs1266108949
• gnomAD v2: 6-162314764-GATCCCATCCA-G
• gnomAD v3: 6-161893732-GATCCCATCCA-G
• gnomAD v4: 6-161893732-GATCCCATCCA-G
• MyVariant Identifiers: chr6:g.162314765_162314774del (hg19) ; chr6:g.161893733_161893742del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.161893733_161893742del , CM000668.2:g.161893733_161893742del	GRCh38
NC_000006.11:g.162314765_162314774del , CM000668.1:g.162314765_162314774del	GRCh37
NC_000006.10:g.162234755_162234764del	NCBI36
NG_008289.1:g.839061_839070del
NG_008289.2:g.839061_839070del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338468.8:c.612+79560_612+79569del	ENSP00000343589.4:n.612+79560_612+79569del
ENST00000366894.6:c.493+79560_493+79569del	ENSP00000355860.2:n.493+79560_493+79569del
ENST00000366898.6:c.734+79560_734+79569del MANE Select	ENSP00000355865.1:n.734+79560_734+79569del
ENST00000673871.1:c.729+79560_729+79569del
ENST00000674436.1:n.370+79560_370+79569del
ENST00000674501.1:n.841+79560_841+79569del
ENST00000338468.7:c.161+79560_161+79569del	ENSP00000343589.3:n.161+79560_161+79569del
ENST00000366892.5:c.734+79560_734+79569del	ENSP00000355858.1:n.734+79560_734+79569del
ENST00000366894.5:c.161+79560_161+79569del	ENSP00000355860.1:n.161+79560_161+79569del
ENST00000366896.5:c.287+79560_287+79569del	ENSP00000355862.1:n.287+79560_287+79569del
ENST00000366897.5:c.650+79560_650+79569del	ENSP00000355863.1:n.650+79560_650+79569del
ENST00000366898.5:c.734+79560_734+79569del	ENSP00000355865.1:n.734+79560_734+79569del
ENST00000479615.5:c.497+79560_497+79569del	ENSP00000434414.1:n.497+79560_497+79569del
NM_004562.2:c.734+79560_734+79569del	NP_004553.2:n.734+79560_734+79569del
NM_013987.2:c.650+79560_650+79569del	NP_054642.2:n.650+79560_650+79569del
NM_013988.2:c.287+79560_287+79569del	NP_054643.2:n.287+79560_287+79569del
XM_011535863.1:c.731+79560_731+79569del	XP_011534165.1:n.731+79560_731+79569del
XM_011535864.1:c.734+79560_734+79569del	XP_011534166.1:n.734+79560_734+79569del
XM_011535865.1:c.734+79560_734+79569del	XP_011534167.1:n.734+79560_734+79569del
XM_017010908.1:c.848+79560_848+79569del	XP_016866397.1:n.848+79560_848+79569del
XM_017010909.2:c.494+79560_494+79569del	XP_016866398.1:n.494+79560_494+79569del
XM_024446449.1:c.497+79560_497+79569del	XP_024302217.1:n.497+79560_497+79569del
XR_001743443.2:n.840+79560_840+79569del
NM_004562.3:c.734+79560_734+79569del MANE Select	NP_004553.2:n.734+79560_734+79569del
NM_013987.3:c.650+79560_650+79569del	NP_054642.2:n.650+79560_650+79569del
NM_013988.3:c.287+79560_287+79569del	NP_054643.2:n.287+79560_287+79569del